Vardenafil Inhaled for Pulmonary Arterial Hypertension PRN Phase 2B Study

PHASE2CompletedINTERVENTIONAL
Enrollment

42

Participants

Timeline

Start Date

September 25, 2020

Primary Completion Date

November 20, 2024

Study Completion Date

January 7, 2025

Conditions
Pulmonary Arterial Hypertension
Interventions
COMBINATION_PRODUCT

Drug: RT234 - vardenafil inhalation powder; Device: Axially Oscillating Sphere dry powder inhaler (AOS DPI)

RT234 capsules of a dry powder formulation containing vardenafil administered via oral inhalation with a non-invasive AOS DPI.

Trial Locations (26)

10029

Mount Sinai Hospital, New York

20010

MedStar Heart and Vascular Institute, Washington D.C.

Mayo Clinic, Rochester

23284

Virginia Commonwealth University, Richmond

27514

University of North Carolina at Chapel Hill, Chapel Hill

29425

Medical University of South Carolina, Charleston

30912

Augusta University, Augusta

35294

University of Alabama, Birmingham

40202

Norton Health, Louisville

43210

The Ohio State University, Columbus

44106

University Hospital, Cleveland

53215

Aurora St. Luke's Medical Center, Milwaukee

63110

Washington University, St Louis

66160

The University of Kansas Medical Center, Kansas City

71103

Ochsner Louisiana State University Health, Shreveport

75246

Baylor Scott and White Institute, Dallas

77030

Houston Methodist Hospital, Houston

78705

Ascension Seton Medical Center Austin, Austin

85724

University of Arizona, Tucson

87131

University of New Mexico, Albuquerque

90024

UCLA, Los Angeles

90033

University of Southern California, Los Angeles

90502

The Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance

94143

University of California San Francisco, San Francisco

95618

UC Davis, Sacramento

02111

Tufts University, Boston

All Listed Sponsors
lead

Respira Therapeutics, Inc.

INDUSTRY

NCT04266197 - Vardenafil Inhaled for Pulmonary Arterial Hypertension PRN Phase 2B Study | Biotech Hunter | Biotech Hunter